Characterization of supernumerary ring marker chromosomes by fluorescence in situ hybridization (FISH). (Q35194867)

7 August 2017

title

Characterization of supernumerary ring marker chromosomes by fluorescence in situ hybridization (FISH). (English)

1 reference

7 August 2017

6

Nordenskjöld M

1 reference

7 August 2017

Blennow E

1

1 reference

7 August 2017

Annerén G

2

1 reference

7 August 2017

Bui TH

3

1 reference

7 August 2017

Berggren E

4

1 reference

7 August 2017

Asadi E

5

1 reference

7 August 2017

publication date

1 August 1993

1 reference

American Journal of Human Genetics

7 August 2017

language of work or name

English

0 references

published in

1 reference

7 August 2017

volume

53

1 reference

7 August 2017

issue

2

1 reference

7 August 2017

page(s)

433-442

1 reference

describes a project that uses

7 August 2017

fluorescence in situ hybridization

1 reference

Outcome of cases of de novo structural rearrangements diagnosed at amniocentesis

inferred from title

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682354

Forty four probands with an additional "marker" chromosome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682354

Supernumary marker chromosomes in a mentally retarded population identified as inv dup(15).

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682354

Extra structurally abnormal chromosomes (ESAC) detected at amniocentesis: frequency in approximately 75,000 prenatal cytogenetic diagnoses and associations with maternal and paternal age

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682354

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682354

The isochromosome 18p syndrome: confirmation of cytogenetic diagnosis in nine cases by in situ hybridization

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682354

Chromosomal in situ suppression hybridization of human gonosomes and autosomes and its use in clinical cytogenetics

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682354

Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682354

Correlation between phenotypic expression of de novo marker chromosomes and genomic organization using replicational banding

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682354

Fluorescence in situ hybridization: applications in cytogenetics and gene mapping

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682354

Chromosomal origin of small ring marker chromosomes in man: characterization by molecular genetics

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682354

Tetrasomy 12p (Pallister-Killian syndrome).

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682354

Chromosome in situ suppression hybridisation in clinical cytogenetics

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682354

Complete characterization of a large marker chromosome by reverse and forward chromosome painting

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682354

A non-isotopic in situ hybridisation study of the chromosomal origin of 15 supernumerary marker chromosomes in man

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682354

Cytogenetic and clinical studies in five cases of inv dup(15)

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682354

Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682354

A chromosome survey of 2,400 normal newborn infants

25 October 2018

1 reference

12 December 2020

Extra marker chromosome in newborn children

1 reference

12 December 2020

C-bands in seven cases of accessory small chromosomes

1 reference

12 December 2020

Prenatal detection of an accessory chromosome identified as an inversion duplication (15)

1 reference

12 December 2020

The genetic significance of accessory bisatellited marker chromosomes

1 reference

12 December 2020

Characterization of the supernumerary chromosome in cat eye syndrome

1 reference

12 December 2020

Marker chromosomes in a series of 10,000 prenatal diagnoses. Cytogenetic and follow-up studies

1 reference

12 December 2020

Evidence for lack of specificity of the DA/DAPI technique

1 reference

12 December 2020

Lack of specificity of DA/DAPI fluorescence

1 reference

12 December 2020

Molecular identification of a small supernumerary marker chromosome by in situ hybridization: diagnosis of an isochromosome 18p with probe L1.84

1 reference

12 December 2020

A study of ten small supernumerary (marker) chromosomes identified by fluorescence in situ hybridization (FISH)

1 reference

12 December 2020

Bisatellited extra small metacentric chromosome in newborns

1 reference

12 December 2020

Identifiers

PMC publication ID

1682354

1 reference

7 August 2017

1 reference